Renström Lina, Stål Per, Song Yafeng, Forsgren Sture
Department of Integrative Medical Biology, Section of Anatomy, Umeå University, Umeå, Sweden.
Perelman School of Medicine & Pennsylvania Muscle Institute, University of Pennsylvania, Philadelphia, PA, USA.
BMC Musculoskelet Disord. 2017 Nov 28;18(1):498. doi: 10.1186/s12891-017-1796-6.
TNF-alpha is suggested to be involved in muscle damage and muscle inflammation (myositis). In order to evaluate whether TNF-alpha is involved in the myositis that occurs in response to muscle overuse, the aim was to examine the expression patterns of TNF receptors in this condition.
A rabbit muscle overuse model leading to myositis in the soleus muscle was used. The expression patterns of the two TNF receptors Tumor Necrosis Factor Receptor type 1 (TNFR1) and Tumor Necrosis Factor Receptor type 2 (TNFR2) were investigated. In situ hybridization and immunofluorescence were utilized. Immunostainings for desmin, NK-1R and CD31 were made in parallel.
Immunoreactions (IR) for TNF receptors were clearly observed in white blood cells, fibroblasts and vessel walls, and most interestingly also in muscle fibers and nerve fascicles in the myositis muscles. There were very restricted reactions for these in the muscles of controls. The upregulation of TNF receptors was for all types of structures seen for both the experimental side and the contralateral nonexperimental side. TNF receptor expressing muscle fibers were present in myositis muscles. They can be related to attempts for reparation/regeneration, as evidenced from results of parallel stainings. Necrotic muscle fibers displayed TNFR1 mRNA and TNFR2 immunoreaction (IR) in the invading white blood cells. In myositis muscles, TNFR1 IR was observed in both axons and Schwann cells while TNFR2 IR was observed in Schwann cells. Such observations were very rarely made for control animals.
The findings suggest that there is a pronounced involvement of TNF-alpha in the developing myositis process. Attempts for reparation of the muscle tissue seem to occur via both TNFR1 and TNFR2. As the myositis process also occurs in the nonexperimental side and as TNF receptors are confined to nerve fascicles bilaterally it can be asked whether TNF-alpha is involved in the spreading of the myositis process to the contralateral side via the nervous system. Taken together, the study shows that TNF-alpha is not only associated with the inflammation process but that both the muscular and nervous systems are affected and that this occurs both on experimental and nonexperimental sides.
肿瘤坏死因子-α(TNF-α)被认为与肌肉损伤和肌肉炎症(肌炎)有关。为了评估TNF-α是否参与因肌肉过度使用而发生的肌炎,本研究旨在检测这种情况下TNF受体的表达模式。
采用建立比目鱼肌肌炎的兔肌肉过度使用模型。研究两种TNF受体,即肿瘤坏死因子受体1型(TNFR1)和肿瘤坏死因子受体2型(TNFR2)的表达模式。采用原位杂交和免疫荧光技术。同时进行结蛋白、神经激肽-1受体(NK-1R)和CD31的免疫染色。
在肌炎肌肉的白细胞、成纤维细胞和血管壁中清晰观察到TNF受体的免疫反应(IR),最有趣的是在肌纤维和神经束中也观察到。在对照肌肉中这些反应非常有限。实验侧和对侧非实验侧所有类型结构的TNF受体均上调。肌炎肌肉中存在表达TNF受体的肌纤维。平行染色结果表明,它们可能与修复/再生的尝试有关。坏死的肌纤维在浸润的白细胞中显示TNFR1 mRNA和TNFR2免疫反应(IR)。在肌炎肌肉中,轴突和雪旺细胞中均观察到TNFR1 IR,而雪旺细胞中观察到TNFR2 IR。对照动物很少有这样的观察结果。
研究结果表明,TNF-α在发展中的肌炎过程中显著参与。肌肉组织的修复似乎通过TNFR1和TNFR2进行。由于肌炎过程也发生在非实验侧,且TNF受体双侧局限于神经束,因此可以推测TNF-α是否通过神经系统参与肌炎过程向对侧的扩散。综上所述,该研究表明TNF-α不仅与炎症过程相关,而且肌肉和神经系统均受到影响,且在实验侧和非实验侧均如此。